CClinicalTrials.gg
CompletedNCT05635253Updated Dec 2, 2022

Influence of Polishing After Bleaching on Color Change and Enamel Morphology

An interventional study of Hydrogen Peroxide 35% and Hydrogen Peroxide 35% + Polishing whitened teeth in Tooth Discoloration, Morphologic Change and Tooth Sensitivity, sponsored by Universidade Federal do Para. Completed at 1 site in Brazil. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-12-02.

Sponsored by Universidade Federal do Para · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Jan 2022, registered Nov 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

This trial evaluated the influence of polishing on enamel color change after in-office bleaching treatment. It also evaluated the influence of polishing on tooth morphology and sensitivity.

02

Conditions studied

  • Tooth Discoloration
  • Morphologic Change
  • Tooth Sensitivity
03

In context

Dentin Sensitivity

282 studies on the registry are indexed under Dentin Sensitivity; 45 are open to participants now.

This study's enrollment of 50 is below the median of 60 across 273 interventional studies indexed under Dentin Sensitivity.

Browse Dentin Sensitivity studies →

Lead sponsor

Universidade Federal do Para is the lead sponsor of 29 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Individuals aged 18 to 30 years old of both sexes;
  • With good oral hygiene;
  • With no sensitivity to tactile and evaporative stimuli;
  • Who have not undergone previous bleaching treatment, and with no caries lesions.

Exclusion criteria

Exclusion Criteria:

  • patients undergoing fixed orthodontic treatment;
  • patients allergic to the bleaching product;
  • drug users or pregnant women;
  • patients with carious lesions, defective restorations and/or periodontal disease, patients with systemic diseases, pulpitis or patients using analgesics.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
50 participants (actual)

Study arms

  • Other
    GROUP GSEM

    In-office whitening treatment with 35% Hydrogen Peroxide

    Other: Hydrogen Peroxide 35%

  • Experimental
    GROUP GP

    In-office whitening treatment with 35% Hydrogen Peroxide + Polishing of whitened teeth

    Other: Hydrogen Peroxide 35% + Polishing whitened teeth

Interventions

  • OtherHydrogen Peroxide 35%

    Group that received only bleaching treatment. Soft tissue protection was performed with a Top Dam light-curing gingival barrier (FGM, Santa Catarina, SC, Brazil). Application of whitening gel (Whitness HP 35%/FGM) on the buccal surface from premolar to premolar in the upper and lower arches. Three 45-minute sessions were held with an interval of seven days between them.

  • OtherHydrogen Peroxide 35% + Polishing whitened teeth

    Group that received only bleaching treatment followed by polishing. Soft tissue protection was performed with a Top Dam light-curing gingival barrier (FGM, Santa Catarina, SC, Brazil). Application of whitening gel (Whitness HP 35%/FGM) on the buccal surface from premolar to premolar in the upper and lower arches. Three 45-minute sessions were held with an interval of seven days between them. After bleaching, the vestibular surfaces were polished for 20s on each bleached tooth, with polishing paste and felt disc (Diamond Flex, FGM, Santa Catarina, SC, Brazil) in low rotation.

06

What researchers measure

Primary outcomes

  1. Influence of polishing on color after tooth whitening

    Color evaluation was performed with the EasyshadeAdvanced spectrophotometer (Vita-Zahnfabrik, GE, Germany)

    Time frame: 14 days

Secondary outcomes

  1. Surface morphology of whitening enamel with and without polishing

    The images were obtained using a electron microscope (Mira3 model) with type electron gun, mounted on supports of aluminum with 12mm of diameter, using tape double adhesive carbon face, and metallic with Au for 2'30'' which deposits about the sample a film thick average of 10 to 15nm. The images were generated by detecting secondary electrons, using a voltage acceleration of 5 kV and a working distance of around 15 mm.

    Time frame: 14 days

  2. Influence of polishing on sensitivity after tooth whitening

    assessment of sensitivity during treatment using a visual analogue scale with values from 0 to 10, with higher values indicating a worse level of pain.

    Time frame: 14 days

07

Study locations

1 site
  • Cecy Martins Silva
    Belém, PA 66075-110, Brazil
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 2, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05635253
Lead sponsor
Universidade Federal do Para
Responsible party
Cecy Martins Silva (Clinical professor, Universidade Federal do Para) — Principal investigator
First posted
Dec 2, 2022
Start date
Jan 10, 2022
Primary completion
Aug 26, 2022
Completion
Sep 12, 2022
Last update
Dec 2, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion